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作 者:李俊[1] 梁君山[1] 周爱武[1] 陈敏珠[1] 徐叔云[1]
机构地区:[1]安徽医科大学临床药理研究所
出 处:《中国药理学与毒理学杂志》1994年第1期53-55,共3页Chinese Journal of Pharmacology and Toxicology
摘 要:白芍总甙(TGP)对脂多糖(LPS)诱导的小鼠脾淋巴细胞增殖反应的量效曲线呈钟形,用贴壁法除去脾细胞中巨噬细胞(MΦ)或加入10μmol·L1吲哚美辛(Ind)可使TGP量效曲线的下降支消失,再加5%同系小鼠腹腔MΦ中或前列腺素E2(PGE2)0.0220μmol·L1可使量效曲线下降支再现.同步检测TGP对LPS诱导大鼠腹腔MΦ产生PGE2与白介素1(IL1).结果表明,TGP0.5-3l2.5μg·mL1对LPS诱导的IL-1产生曲线呈钟形.而TGPLPS的PGE2产生曲线呈浓度依赖性地增高;在12.5-312.5μg·mLTGP范围内,10μmol·L1Ind可使高浓度TCPLPS的IL-1释放曲线明显抬高。提示TGP对LPS诱导的B细胞增殖反应和IL-1诱生的负调节作用都与其促进MΦ释放PGE2有关.The negatively regulatory mecha-nisms of total glucosides of paeony(TGP) on lipo-polysaccharide(LPS)-induced lymphocyte proliferation in mouse spleen and interleukin 1(IL-1) pro-duction of rat peritoneal macrophages(M)were stu-died. The descending limb of concentration-effectcurve of splenocyte proliferation disappeared whenindometacin(Ind,10 umol·L1) was added orM was depleted from the cuIture and reappearedWhen 5% of M or prostaglandin E2(PGE2,0.02-20umol·L1) was added again. The results suggestedthat the negatively regulatory effects of TGP onLpS induced proliferation of splenocytes in mice weremediated by the PGE2 production of M.The effects of TGP on LPS-induccd IL-1andPCE2 prduction from rat M were studiedsimultaneously. The production curve of IL-1 seemsto be bell-shaped,but that of PGE2 was enhanced bvTGP(0.5-312.5 mg·L1)The results suggested thatthe negatively regulatory effect of TGP on LPS-in-duced IL-1 production was also mediated by thePGE2 production of M.
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